Evidence map›Paper›PMID 40384217›Full record

ArticleJournal of veterinary internal medicine

Effect of Fenofibrate on Markers of Gut Barrier Function in Dogs With Naturally Occurring Diabetes Mellitus.

Allison L O'Kell, Jocelyn Mott, Lauren Porter, Chiquitha D Crews, Yu-An Wu, Rosemary Walzem, Joerg M Steiner, Chen Gilor

Abstract read
In one paragraph

Article in Journal of veterinary internal medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Allison L O'KellDepartment of Small Animal Clinical Sciences, University of Florida, Gainesville, Florida, USA.
Jocelyn MottDepartment of Small Animal Clinical Sciences, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0002-2176-9287
Lauren PorterDepartment of Small Animal Clinical Sciences, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0009-0002-0015-3237
Chiquitha D CrewsDepartment of Small Animal Clinical Sciences, University of Florida, Gainesville, Florida, USA.
Yu-An WuGastrointestinal Laboratory, Department of Small Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas, USA.ORCID https://orcid.org/0000-0003-0792-2414
Rosemary WalzemDepartment of Poultry Sciences, Graduate Faculty of Nutrition, Texas A&M University, College Station, Texas, USA.
Joerg M SteinerGastrointestinal Laboratory, Department of Small Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas, USA.ORCID https://orcid.org/0000-0003-3336-2086
Chen GilorDepartment of Small Animal Clinical Sciences, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0003-0393-4135

Funding

American Kennel Club Canine Health Foundation 02850-A
6 · The paper itself

Abstract

backgroundFenofibrate improves gut barrier function and reduces serum lipids in purpose-bred dogs with induced diabetes mellitus (DM), but its effects in dogs with naturally occurring DM are unknown.

objectivesDetermine the effects of fenofibrate on markers of systemic and pancreatic inflammation, markers of gut barrier function, lipoprotein profiles, and glycemic control in dogs with naturally occurring DM. ANIMALS: Sixteen client-owned dogs with naturally occurring, uncomplicated DM.

methodsLongitudinal cohort study. Dogs were treated with fenofibrate (Tricor, 6-10 mg/kg, P.O., once daily) for 21 days. Interstitial glucose, serum cytokines, lipopolysaccharide (LPS), pancreatic lipase, and lipid profiles were compared between baseline and day 21 using paired t-tests and Wilcoxon signed-rank tests.

resultsFenofibrate had no effect on glycemic control, serum cytokines, or serum pancreatic lipase. Compared to baseline, the concentrations of serum LPS decreased at day 21 by (mean ± SD) 15 ± 24% (95% CI 2-28%, p = 0.03), serum triglycerides decreased by 36 ± 39% (95% CI 15-56%, p = 0.002), and serum cholesterol decreased by 20 ± 14% (95% CI 12-28%, p < 0.0001). CONCLUSIONS AND CLINICAL IMPORTANCE: Fenofibrate treatment was not associated with a decrease in markers of systemic or pancreatic inflammation. In diabetic dogs, short-term fenofibrate treatment appears to be safe, and the improvement in gut barrier function and lipid profiles might lead to long-term benefits, such as reduction in pancreatitis risk and frequency of signs of gastrointestinal disease.

Indexed as

Diabetes MellitusDog DiseasesFenofibrateHypolipidemic AgentsAnimalsBiomarkersBlood GlucoseCytokinesDogsFemaleLipaseLipopolysaccharidesLongitudinal StudiesMaleBiomarkersBlood GlucoseCytokinesFenofibrateHypolipidemic AgentsLipaseLipopolysaccharidesfibroblast growth factor‐21lipopolysaccharidepancreatic lipase immunoreactivitypancreatitisperoxisome proliferator‐activated receptor

Identifiers

PMID40384217
PMCPMC12086328

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.